Skip Navigation

American Zoologist 2001 41(3):430-441; doi:10.1093/icb/41.3.430
© 2001 by The Society for Integrative and Comparative Biology
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Request Permissions
Google Scholar
Right arrow Articles by Borst, D. W.
Right arrow Articles by Holford, K. C.
Right arrow Search for Related Content
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?


Regulation of the Crustacean Mandibular Organ1

David W. Borst2,1, Jeff Ogan1, Brian Tsukimura1, Todd Claerhout1 and Kenneth C. Holford1
1 Department of Biological Sciences, Illinois State University, Normal, Illinois 61790-4120

The crustacean mandibular organ (MO) produces methyl farnesoate (MF), a juvenile hormone-related compound thought to have roles in crustacean reproduction and development. Therefore, the control of MF production by the MO has been of considerable interest. Current evidence indicates that the MO is negatively regulated by peptides present in the eyestalk (MO inhibiting factor, MO-IH). Several eyestalk neuropeptides have been identified that inhibit MF synthesis by MO incubated in vitro. The amino acid sequences of these MO-IH peptides are similar to peptides in the crustacean hyperglycemic hormone (CHH) family of neuropeptides. In addition, there appears to be a compound in the eyestalk that lowers hemolymph levels of MF in vivo but does not directly affect the MO in vitro. The inhibition of MF synthesis by eyestalk peptides involves the inhibition of farnesoic acid O-methyl transferase, the last enzyme in the MF biosynthetic pathway. The activity of this enzyme is affected by cyclic nucleotides, suggesting that these compounds may be involved in the signal transduction pathway mediating the effects of MO-IH.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.